Allele Registry

Canonical Allele Identifier: PA2827018708

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000221766

RCV001341323

RCV002251447

ClinVar Variation:

233995

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305761.1:p.Ser1061Trp	CA045126 NM_001318832.2:c.3182C>G